Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Aluminum oxide coated hafnium/nitrogen co-doped lithium iron phosphate positive electrode material and preparation method thereof

A technology of lithium iron phosphate and positive electrode material, applied in chemical instruments and methods, phosphates, phosphorus oxyacids, etc., can solve the problems of low ion conductivity and electron conductivity of lithium iron phosphate, low rate discharge and other performance and production costs. Satisfy and hinder the large-scale application of materials, etc., to achieve the effect of improving electrochemical performance, huge economic value and environmental protection value, and low manufacturing cost

Pending Publication Date: 2020-07-10
SHANDONG GOLDENCELL ELECTRONICS TECH
View PDF7 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the problem at this stage is that the ion conductivity and electronic conductivity of lithium iron phosphate are relatively low, which is only suitable for charging and discharging at low current density. High-rate charging and discharging will reduce the specific capacity. Large-scale application in more fields
[0004] Although many modification methods have been developed at this stage, the prepared lithium iron phosphate materials cannot meet the needs of industrialization in terms of energy density, cycle performance, rate discharge and production costs.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Aluminum oxide coated hafnium/nitrogen co-doped lithium iron phosphate positive electrode material and preparation method thereof
  • Aluminum oxide coated hafnium/nitrogen co-doped lithium iron phosphate positive electrode material and preparation method thereof
  • Aluminum oxide coated hafnium/nitrogen co-doped lithium iron phosphate positive electrode material and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] At room temperature, weigh Hf(NO 3 ) 4 , lithium carbonate, diammonium hydrogen phosphate, and ferrous sulfate heptahydrate were added to deionized water to disperse and stir to prepare a dispersion liquid, wherein the stirring time was selected to be 10 hours, and the stirring rate was 1500 rpm. The obtained dispersion liquid was evaporated to dryness by rotary evaporation, the rotary evaporation temperature was 70° C., and the rotational speed was 100 rpm. Afterwards, the dried mixture was calcined in a tube furnace at a temperature of 500°C for 10 hours at a heating rate of 1°C / min to obtain a lithium iron phosphate precursor. The obtained lithium iron phosphate precursor is placed again in the mixed solution of aluminum nitrate, urea and glucose, the molar ratio of aluminum nitrate, urea and glucose is 0.1:5:1, the quality of lithium iron phosphate precursor and aluminum nitrate, The ratio of the mass sum of urea and glucose is 1:2, the rapid stirring speed is 120...

Embodiment 2

[0030] At room temperature, weigh HfCl according to the molar ratio of 0.2:1:1:1 4, lithium nitrate, diammonium hydrogen phosphate, and ferrous sulfate heptahydrate were added to deionized water to disperse and stir to prepare a dispersion liquid, wherein the stirring time was selected to be 20 hours, and the stirring rate was 900 rpm. The obtained dispersion liquid was evaporated to dryness by rotary evaporation, the rotary evaporation temperature was 70° C., and the rotational speed was 100 rpm. Afterwards, the dried mixture was calcined in a tube furnace at a temperature of 600°C for 8 hours at a heating rate of 2°C / min to obtain a lithium iron phosphate precursor. The obtained lithium iron phosphate precursor is placed back in the mixed solution of aluminum nitrate, urea and glucose, the molar ratio of aluminum nitrate, urea and glucose is 0.15:5:1, the quality of lithium iron phosphate precursor and aluminum nitrate, The ratio of the mass sum of urea and glucose is 1:2, ...

Embodiment 3

[0032] At room temperature, weigh HfCl according to the molar ratio of 0.15:1:1:1 4 , lithium nitrate, phosphoric acid, and ferric chloride were added into deionized water to disperse and stir to prepare a dispersion liquid, wherein the stirring time was selected to be 20 hours, and the stirring rate was 900 rpm. The obtained dispersion liquid was evaporated to dryness by rotary evaporation, the rotary evaporation temperature was 70° C., and the rotational speed was 100 rpm. Afterwards, the dried mixture was calcined in a tube furnace at a temperature of 700°C for 5 hours at a heating rate of 3°C / min to obtain a lithium iron phosphate precursor. The obtained lithium iron phosphate precursor is placed back in the mixed solution of aluminum nitrate, urea and glucose, the molar ratio of aluminum nitrate, urea and glucose is 0.15:6:1.5, the quality of lithium iron phosphate precursor is the same as that of aluminum nitrate, The ratio of the mass sum of urea and glucose is 1:2, th...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

Firstly, four raw materials, namely hafnium salt, a lithium source, a phosphorus source and an iron source, are mixed and subjected to heat treatment to obtain hafnium-doped lithium iron phosphate; secondly, the lithium iron phosphate precursor is re-placed into a mixed solution of aluminum nitrate, urea and glucose for secondary dispersion and mixing, and hydrothermal reaction is performed; and finally, the hydrothermal product is cleaned, dried and calcined to obtain the aluminum oxide coated hafnium / nitrogen co-doped lithium iron phosphate positive electrode material. The method has the advantages of simple process steps, short flow, adjustable morphology and structure and the like in the aspect of preparing the lithium iron phosphate positive electrode material. The prepared lithium iron phosphate positive electrode material has obvious advantages in the aspects of high-rate performance, cycle index, energy density and other electrochemical properties, the performance is more stable, the equipment requirement of the whole route is low, the process stability is good, and the material has important industrial popularization and application value.

Description

technical field [0001] The invention relates to the technical field of positive electrode materials for lithium ion batteries, and relates to an aluminum oxide-coated nitrogen / aluminum co-doped lithium iron phosphate positive electrode material and a preparation method thereof. Background technique [0002] Lithium-ion batteries have the advantages of high specific energy, high power density, and long cycle life, and are widely used in electric vehicles, notebook computers, camcorders, and other electric equipment. In recent years, special equipment fields such as space flight devices and deep-sea diving equipment have also raised an urgent need for the use of lithium-ion batteries to provide durable power output. Lithium-ion cathode materials have a decisive impact on the energy density of lithium-ion batteries, which are generally lithium-containing variable-valence metal compounds. Currently widely used cathode materials for lithium-ion batteries mainly include lithium-r...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): H01M4/36H01M4/48H01M4/46H01M4/58H01M10/0525H01M10/42C01B25/26C01B25/45C01B25/37
CPCH01M4/366H01M4/48H01M4/463H01M4/5825H01M10/0525H01M10/4235C01B25/26C01B25/45C01B25/375Y02E60/10
Inventor 薛娟娟张敬捧王勇
Owner SHANDONG GOLDENCELL ELECTRONICS TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products